A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17154570



Internal ID21494606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:81080270..81080455hg38UCSC Ensembl
chr7:80709586..80709771hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38186
hg19186
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5569635
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17154570
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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